HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → 6-Methoxy-7-(3-morpholinopropoxy)-3,4-dihydroquinazolin-4-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Methanol | HCID 887 | — |
| Reactant | 6-Methoxy-7-(3-morpholinopropoxy)-3-pivaloyloxymethyl-3,4-dihydroquinazolin-4-one | HCID 22732276 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 6-Methoxy-7-(3-morpholinopropoxy)-3,4-dihydroquinazolin-4-one | HCID 135437116 | — |
Reaction Steps
6-Methoxy-7-(3-morpholinopropoxy)-3-pivaloyloxymethyl-3,4-dihydroquinazolin-4-one (1.85 g) was stirred in methylene chloride (20 ml) and methanol (20 ml) and methanolic ammonia (2M, 100 ml) was added. The reaction was stirred at ambient temperature for 48 hours, evaporated to dryness, and then stirred in diethyl ether for 1 hour. The reaction mixture was filtered affording 6-methoxy-7-(3-morpholinopropoxy)-3,4-dihydroquinazolin-4-one as a solid, (1.22 g, 90%); NMR: 1.9 (m, 2H), 2.4 (broad m, 6H), 3.55 (m, 4H), 3.88 (s, 3H), 4.12 (m, 2H), 7.1 (s, 1H), 7.41 (s, 1H), 7.94 (s, 1H); m/s: M+H+ 320.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06593333B1 |
| Source dataset | uspto-grants-2003_07 |
| ORD ID | ord-bae445f080054001bde75c8d55764e3e |
| Source note | uspto-grants-2003_07 |